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Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Capillary malformation - arteriovenous malformation
1 OMIM reference -
1 associated gene
No signs/symptoms info
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Capillary malformation - arteriovenous malformation

CBFB
(UniProt - OMIM)
 RASA1
(UniProt - OMIM)
FLT3
(UniProt - OMIM)
KIT
(UniProt - OMIM)
MYH11
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
KIT
(0.83)
RASA1


Citations in the biomedical literature:


Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
CBFB FLT3 KIT MYH11
Capillary malformation - arteriovenous malformation
RASA1



Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Capillary malformation - arteriovenous malformation

Synonym(s):
(no synonyms)

Synonym(s):
- CM-AVM
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.